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Updated: May 24, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Pharmacokinetic approach for optimizing gentamicin use in neonates during the first week of life
Ahmed S Ali1, M Fadulallah Farouq, Khalid A Al-Faify
1Department of Pharmacology, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia. Ahmedshaker21@yahoo.com
Insights
Optimizing gentamicin use in neonates is crucial for treating sepsis. A dose of 4.5 mg/kg every 36 hours is recommended for most newborns, with adjustments for extremely low birth weight infants.
Area of Science:
- Neonatal pharmacology
- Pediatric infectious diseases
- Clinical pharmacokinetics
Background:
- Gentamicin is a critical antibiotic for treating neonatal sepsis.
- Optimizing gentamicin dosing in the first week of life is essential for efficacy and safety.
Purpose of the Study:
- To optimize gentamicin dosage and interval for neonates during their first week of life.
- To evaluate the pharmacokinetic parameters of gentamicin in a neonatal population.
Main Methods:
- Seventy-three neonates receiving gentamicin (4-5 mg/kg, 24-48 hr interval) were studied.
- Peak and trough serum levels were measured; pharmacokinetic parameters were estimated.
- Statistical analysis used ANOVA with SPSS Version 13.
Main Results:
- 73% achieved therapeutic peak gentamicin levels (6-12 μg/ml).
- 12% had potentially toxic trough levels (>2 μg/ml), more frequent with 24 hr dosing.
- Higher volume of distribution observed in neonates with sepsis; longer half-life in extremely low birth weight infants.
Conclusions:
- A gentamicin dose of 4.5 mg/kg every 36 hours is recommended for neonates with normal or low birth weight.
- An every 48-hour interval is suggested for extremely low birth weight neonates.
Introduction:
Gentamicin is an essential drug for the treatment of sepsis in neonates. The current work aims to optimize the use of gentamicin in neonates during the first week of life.
Materials And Methods:
The study was done at King Abdul-Aziz university hospital. Seventy-three neonates who received gentamicin 4-5 mg/kg and dosing interval at 24-48 hr were enrolled. Peak and trough serum levels of gentamicin were determined by immunoassay. Pharmacokinetic parameters were estimated assuming one compartment model and first order elimination kinetic. Analysis of variance was used to test the difference between means using Statistical Package for the Social Sciences (SPSS) Version 13.
Results:
About 73% of the patients attained peak gentamicin level within therapeutic range (6-12μg/ml), while 12% showed potentially toxic trough level (>2 μg /ml). The incidence of trough level was higher among patients receiving the drug every 24 hr. There was no clear correlation between high trough level and serum creatinine. High volume of distribution (Vd) of gentamicin (0.40-0.45) L/kg was observed. Neonates with proven sepsis showed higher mean Vd. Those with extremely low birth weight showed significantly longer half life of 11.5 h. Other neonates showed half life of (8-9) hr.
Conclusions:
Gentamicin dose of 4.5 mg/kg every 36 hr is recommended as simple empirical regimen during the 1(st) week of life for neonates with normal or LBW and every 48 hr for those with ELBW.
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